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botiss Jason® membrane - HSA Registration DE0508289

Access comprehensive regulatory information for botiss Jason® membrane in the Singapore medical device market through Pure Global AI's free database. This CLASS D medical device is registered under HSA registration number DE0508289 and owned by botiss biomaterials GmbH. The device was registered on July 13, 2023.

This page provides complete registration details including product owner information, registrant details, importer information, and regulatory compliance data from the official Singapore HSA medical device database. Pure Global AI offers free access to Singapore's complete medical device registry, helping global MedTech companies navigate HSA regulations efficiently.

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CLASS D
DE0508289
botiss Jason® membrane
HSA Registration Number: DE0508289
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Product Description

Jason® membrane is a completely resorbable collagen membrane to be used in stomatology and maxillo-facial surgery, implantology, periodontology, oral surgery and endodontology to support guided tissue and bone regeneration (GTR and GBR), and for covering bone grafts and dental implants.

Device Classification
Device Class
CLASS D
Medical Speciality Area
Dental
Registration Information
Registration Number
DE0508289
Registration Date
July 13, 2023
Change Notification Approval Date
February 18, 2025
Retention Due Date
July 12, 2025
Product Owner
Short Name
botiss biomaterials GmbH
Address
Hauptstr. 28, 15806 Zossen, GERMANY
Registrant
Address
250 NORTH BRIDGE ROAD, RAFFLES CITY TOWER, #19-05, SINGAPORE 179101
Importer
Address
250 NORTH BRIDGE ROAD, RAFFLES CITY TOWER, #19-05, SINGAPORE 179101
Model Information
Model Name(s)
Jason® Membrane Jason® Membrane Jason® Membrane
Model Identifier(s)
BO-681520 BO-682030 BO-683040